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57855-22-8

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57855-22-8 Usage

Physical state

Colorless liquid

Odor

Strong, pungent

Usage

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Role in organic chemistry

Reagent for introducing the bromine atom onto a carbon-carbon double bond

Additional uses

Cross-linking agent in polymers, solvent in various industrial processes

Hazardous nature

Considered a hazardous chemical

Handling precautions

Should be handled with caution due to potential health and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 57855-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,5 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57855-22:
(7*5)+(6*7)+(5*8)+(4*5)+(3*5)+(2*2)+(1*2)=158
158 % 10 = 8
So 57855-22-8 is a valid CAS Registry Number.

57855-22-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-1-HEXENE

1.2 Other means of identification

Product number -
Other names n-hexen-1-ylbromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57855-22-8 SDS

57855-22-8Relevant articles and documents

Practical regio- and stereoselective azidation and amination of terminal alkenes

Ojo, Olatunji S.,Miranda, Octavio,Baumgardner, Kyle C.,Bugarin, Alejandro

, p. 9354 - 9358 (2019/01/03)

There is significant interest in developing more rapid and efficient production of nitrogen-containing allylic compounds, as widely used in various syntheses. This work reports a variety of allylic azides and allylic amines synthesized by an efficient, new one-pot protocol that employs readily available terminal alkenes as starting materials. This method is highly regio- and stereoselective, affording the linear (E)-isomer, under metal-free conditions. This process tolerates several functional groups including halogen-containing molecules; it is general for azides and amine nucleophiles; and, adducts were obtained in good yields.

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